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Valeriana microphylla

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404f869afd3798028891
Scientific name Valeriana microphylla
Authority Kunth
First published in Nov. Gen. Sp. 3: 325 (1819)

Ethnobotanical Use Top

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General Uses Top

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Common products:
No documented commercial or industrial products are reported for Valeriana microphylla (Kunth).

Industrial and craft applications:
No documented uses.

Food and beverages (non-medicinal):
No documented uses.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
No documented properties relevant to commercial or industrial use.

Standards and regulation:
No established standards or regulatory frameworks are reported for products derived from this taxon.

Sustainability and sourcing:
No reported sustainable sourcing initiatives for this taxon.

Synonyms Top

Scientific name Authority First published in
Valeriana alophis Graebn. Bot. Jahrb. Syst. 26: 432 (1899)
Valeriana amphilophis Graebn. Bot. Jahrb. Syst. 26: 433 (1899)
Valeriana gonatolophis Graebn. Bot. Jahrb. Syst. 26: 432 (1899)
Valeriana hieronymii Graebn. Bot. Jahrb. Syst. 26(3-4): 431. 1899 [31 Jan 1899]
Valeriana origanifolia Turcz. Bull. Soc. Imp. Naturalistes Moscou 25(II): 171 (1852)
Valeriana bonplandiana Wedd. Chlor. Andina 2: 19. 1859 [1857 publ. 7 Mar 1859]
Valeriana revoluta Diels Biblioth. Bot. 116: 155 (1937)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001143867
Tropicos 33500229
KEW urn:lsid:ipni.org:names:286639-2
The Plant List tro-33500229
Open Tree Of Life 21453
NCBI Taxonomy 243116
IPNI 286639-2
iNaturalist 778004
GBIF 4095247
EOL 5236598
CMAUP NPO22892

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Chemical Constituents, Enantiomer Content, Antioxidant and Anticholinesterase Activities of Valeriana microphylla Kunth Essential Oil Aguilar G, Calva J, Cartuche L, Salinas M, Armijos C Plants (Basel) 30-May-2023
PMCID:PMC10255249
doi:10.3390/plants12112155
PMID:37299143
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Ethnobotany of Indigenous Saraguros: Medicinal Plants Used by Community Healers “Hampiyachakkuna” in the San Lucas Parish, Southern Ecuador Andrade JM, Lucero Mosquera H, Armijos C Biomed Res Int 04-Jul-2017
PMCID:PMC5514338
doi:10.1155/2017/9343724
PMID:28744470
Strong upslope shifts in Chimborazo's vegetation over two centuries since Humboldt Morueta-Holme N, Engemann K, Sandoval-Acuña P, Jonas JD, Segnitz RM, Svenning JC Proc Natl Acad Sci U S A 14-Sep-2015
PMCID:PMC4611603
doi:10.1073/pnas.1509938112
PMID:26371298
Adaptation and Convergent Evolution within the Jamesonia-Eriosorus Complex in High-Elevation Biodiverse Andean Hotspots Sánchez-Baracaldo P, Thomas GH PLoS One 23-Oct-2014
PMCID:PMC4207698
doi:10.1371/journal.pone.0110618
PMID:25340770
Valtrates and Lignans in Valeriana microphylla. Bach KK, Ghia F, Torssell KB Planta Med 01-Oct-1993
doi:10.1055/S-2006-959740
PMID:17236012

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1055/S-2006-959740
3,6-Bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol 13824420 Click to see 374.40 unknown https://doi.org/10.1055/S-2006-959740
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see 358.40 unknown https://doi.org/10.1055/S-2006-959740
8-Hydroxypinoresinol 3010930 Click to see 374.40 unknown https://doi.org/10.1055/S-2006-959740
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1055/S-2006-959740
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
[(1R,4aS,6R,7S,7aS)-4-(acetyloxymethyl)-1-(3-methylbutanoyloxy)spiro[4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-6-yl] 3-methylbutanoate 162870557 Click to see 424.50 unknown https://doi.org/10.1055/S-2006-959740
[(1R,6S,7R,7aR)-4-(acetyloxymethyl)-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-6-yl] 3-methylbutanoate 124566783 Click to see CC(C)CC(=O)OC1C=C2C(C13CO3)C(OC=C2COC(=O)C)OC(=O)CC(C)C 422.50 unknown https://doi.org/10.1055/S-2006-959740
[(1R,6S,7R,7aR)-6-acetyloxy-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-4-yl]methyl 3-methylbutanoate 163024903 Click to see 422.50 unknown https://doi.org/10.1055/S-2006-959740
[(1R,6S,7R,7aR)-6-acetyloxy-4-(acetyloxymethyl)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-1-yl] 3-methylbutanoate 162914435 Click to see 380.40 unknown https://doi.org/10.1055/S-2006-959740
[(1S,4aS,6R,7R,7aS)-6-hydroxy-7-methyl-1-(3-methylbutanoyloxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 162951957 Click to see 368.50 unknown https://doi.org/10.1055/S-2006-959740
[(4aR,7R,7aS)-6-acetyloxy-1-(3-methylbutanoyloxy)spiro[4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-4-yl]methyl 3-methylbutanoate 137796089 Click to see CC(C)CC(=O)OCC1=COC(C2C1CC(C23CO3)OC(=O)C)OC(=O)CC(C)C 424.50 unknown https://doi.org/10.1055/S-2006-959740
[6-acetyloxy-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-4-yl]methyl 3-methylbutanoate 10477321 Click to see 422.50 unknown https://doi.org/10.1055/S-2006-959740
[6-acetyloxy-4-(acetyloxymethyl)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-1-yl] 3-methylbutanoate 162914434 Click to see 380.40 unknown https://doi.org/10.1055/S-2006-959740
[6-Hydroxy-7-methyl-1-(3-methylbutanoyloxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-yl]methyl 3-methylbutanoate 78174200 Click to see 368.50 unknown https://doi.org/10.1055/S-2006-959740
Butanoic acid, 3-methyl-, 4-((acetyloxy)methyl)-4a,5,6,7a-tetrahydrospiro(cyclopenta(c)pyran-7(1H),2'-oxirane)-1,6-diyl ester 147184 Click to see 424.50 unknown https://doi.org/10.1055/S-2006-959740
Diavaltrate 101656903 Click to see 380.40 unknown https://doi.org/10.1055/S-2006-959740
Didrovaltrate 65689 Click to see CC(C)CC(=O)OCC1=COC(C2C1CC(C23CO3)OC(=O)C)OC(=O)CC(C)C 424.50 unknown https://doi.org/10.1055/S-2006-959740
Isovaltrate 92275 Click to see 422.50 unknown https://doi.org/10.1055/S-2006-959740
Nardostachin 196699 Click to see 368.50 unknown https://doi.org/10.1055/S-2006-959740
Valepotriate 537344 Click to see 422.50 unknown https://doi.org/10.1055/S-2006-959740
Valtrate 442436 Click to see 422.50 unknown https://doi.org/10.1055/S-2006-959740
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aR,6bS,8aS,9R,10S,12aS,14aS,14bS)-10-hydroxy-2,2,4a,6a,6a,8a,9,14a-octamethyl-3,4,6,6b,7,8,9,10,11,12,12a,13,14,14b-tetradecahydro-1H-picen-5-one 101679786 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,9,10,12,12a,13,14,14b-tetradecahydropicene-3,8-dione 21636453 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
(Z,6S)-2-methyl-6-[(5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 51693592 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
3-Epioleanolic acid 11869658 Click to see 456.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,6R,7R,7aS)-4-(acetyloxymethyl)-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-6-yl] 3-acetyloxy-3-methylbutanoate 162844481 Click to see 480.50 unknown https://doi.org/10.1055/S-2006-959740
[(7R,7aS)-4-(acetyloxymethyl)-1-(3-methylbutanoyloxy)spiro[6,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-oxirane]-6-yl] 3-acetyloxy-3-methylbutanoate 137706187 Click to see 480.50 unknown https://doi.org/10.1055/S-2006-959740
4-[(Acetyloxy)methyl]-1-[(3-methylbutanoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl 3-(acetyloxy)-3-methylbutanoate 22245467 Click to see CC(C)CC(=O)OC1C2C(=CC(C23CO3)OC(=O)CC(C)(C)OC(=O)C)C(=CO1)COC(=O)C 480.50 unknown https://doi.org/10.1055/S-2006-959740
Acevaltrate 65717 Click to see CC(C)CC(=O)OC1C2C(=CC(C23CO3)OC(=O)CC(C)(C)OC(=O)C)C(=CO1)COC(=O)C 480.50 unknown https://doi.org/10.1055/S-2006-959740
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Podocarpusflavone A 5320644 Click to see 552.50 unknown via CMAUP database
Podocarpusflavone B 5320646 Click to see 566.50 unknown via CMAUP database

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